Canonical Allele Identifier: CA2650261214
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454230C>G , CM000663.2:g.207454230C>G GRCh38
NC_000001.10:g.207627575C>G , CM000663.1:g.207627575C>G GRCh37
NC_000001.9:g.205694198C>G NCBI36
NG_013006.1:g.4931C>G , LRG_348:g.4931C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1135C>G ENSP00000514493.1:n.-385+1135C>G
ENST00000367057.7:c.-189C>G ENSP00000356024.3:n.-189C>G
ENST00000367058.7:c.-189C>G ENSP00000356025.3:n.-189C>G
ENST00000367059.3:c.-189C>G ENSP00000356026.3:n.-189C>G